| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45769192-45769329 | Rare:40 | ||||
| chr19:46346938-46347099 | Common:3; Rare:51 | ||||
| chr19:46600913-46601076 | Common:2; Rare:66 | ||||
| chr19:46601188-46601420 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chr19:46787450-46787579 | Rare:35 | ||||
| chr19:46788586-46788877 | Common:2; Rare:64 | ||||
| chr19:47112146-47112335 | Rare:52 | ||||
| chr19:47112538-47112657 | Common:2; Rare:28 | ||||
| chr19:47256460-47256577 | Rare:45 | ||||
| chr19:47778400-47778748 | Common:2; Rare:113 | ||||
| chr19:48170262-48170706 | Common:2; Rare:120 | ||||
| chr19:48321345-48321485 | Common:1; Rare:37 | ||||
| chr19:48325261-48325573 | Common:2; Rare:72 | ||||
| chr19:48390886-48390970 | Rare:7 | ||||
| chr19:48445881-48446028 | Rare:54 |